Clinical Product Manager – VeriSight 3D ICE (Intracardiac Echo) (Plymouth MN or Cambridge MA)

Philips•Plymouth, MA

1d•Hybrid

About The Position

This role integrates clinical expertise into product development, executes the ICE (Intracardiac Echo) data strategy and clinical testing and validation, and drives effective commercialization and adoption through asset creation and workflow dissemination. The position involves leading and supporting AI data collection, serving as a clinical subject matter expert, driving external clinical validation, and providing clinical leadership for studies. The successful candidate will support product launch and post-launch activities, contribute to marketing asset development, and maintain oversight of the clinical image library. This role offers a significant impact in the emerging field of 3D ICE-guided interventions and an opportunity to grow into a leading clinical voice in the high-growth intracardiac echocardiography business within Philips.

Requirements

3+ years of experience in interventional cardiac sonography
RDCS/RCS Certification
Ability to successfully perform the minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position

Nice To Haves

ICE interventional guidance in structural heart disease and/or electrophysiology
Stakeholder Management
Clinical Research
New Product Introduction (NPI)
Clinical & Medical Affairs Know-how
Product Lifecycle Management
Ultrasound Technology Acumen
Feedback Management
Bachelor’s degree in business administration, Marketing, Engineering, Product Management or equivalent

Responsibilities

Lead and support AI data collection, annotation, governance, and lifecycle management from a clinical perspective, ensuring data relevance, quality, traceability, and ethical use.
Work closely with data science and engineering teams to align datasets with clinical use cases, claims strategy, and regulatory expectations.
Ensure site selection, management, and training in collaboration with clinical development and clinical operations teams.
Serve as a clinical subject matter expert within the Advanced Development (AD) and Product Development Lifecycle Management (PDLM) frameworks, providing clinical guidance from concept through launch.
Ensure and safeguard clinical integrity, usability, and impact of ICE innovations.
Drive and execute external clinical validation and claims definition for new product introductions.
Provide clinical leadership and support for clinical studies, including feasibility input, protocol review, endpoint definition, and alignment with HEMAR strategy, product claims, regulatory needs, and downstream marketing and commercialization objectives.
Support product launch and post-launch activities by leading the dissemination of workflow training, scientific messaging, objection handling, and clinical differentiation definition.
Ensure consistent application across programs and geographies to enable scalable adoption towards standard of care.
Contribute to the development and maintenance of selected marketing assets, ensuring clinical accuracy and consistency across product messaging.
Maintain oversight of the clinical image library, ensuring appropriate labeling, traceability, compliance, and alignment with approved claims and use cases.